Triflic Anhydride-Mediated Cycloacylation of [60]Fullerene with 1-Naphthoic Acids: Synthesis and Derivatization of [60]Fullerene-Fused Dihydrophenalenones
An efficient triflic anhydride-mediated synthesis of [60]fullerene (C<sub>60</sub>)-fused dihydrophenalenones from C<sub>60</sub> and 1-naphthoic acids has been developed, representing the first one-step construction of C<sub>60</sub>-fused polyaromatic ketones under metal-free conditions. In addition, the C<sub>60</sub>-fused dihydrophenalenones can be reduced to C<sub>60</sub>-fused dihydrophenalenes and C<sub>60</sub>-fused dihydrophenalenols. The structures of the products were unambiguously established by single-crystal X-ray diffraction. A possible reaction mechanism is proposed based on control experiments. Furthermore, a representative C<sub>60</sub>-fused dihydrophenalenone was employed as a third component in organic solar cells, leading to improved device performance.
Authors
- Chong Niu
- Zheng‐Chun Yin (ORCID: https://orcid.org/0000-0002-0311-6688)
- Wen-Jie Qiu (ORCID: https://orcid.org/0000-0002-9880-719X)
- Xinmin Huang
- Zhiwei Xu
- Guan-Wu Wang
Institutions
- University of Science and Technology of China (CN)
- State Key Laboratory of Chemical Engineering (CN)
- Anhui Normal University (CN)
- Lanzhou University (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2026-03-16
- DOI
- https://doi.org/10.1021/acs.orglett.6c00679
- Primary Topic
- Fullerene Chemistry and Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.00